Autoinflammation – Eine klinische und genetische Herausforderung

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

In the last two decades clinical rheumatological practice has been confronted with a steadily increasing number of autoinflammatory diseases, the immunological pathomechanisms of which have been elucidated and in part can be clinically well classified. Whereas targeted genetic diagnostics previously served to confirm a clinically suspected diagnosis, genetic sequencing technology has much improved and enables a new diagnostic approach via high-throughput sequencing, e.g., panel sequencing, whole exome and whole genome sequencing. Thus, the decision to make a diagnosis clinically and/or genetically, has become a daily challenge. This article contrasts the clinical, immunological and genetic aspects of autoinflammatory diseases.
Translated title of the contribution
Autoinflammation—A clinical and genetic challenge

Details

Original languageGerman
Pages (from-to)953–965
Number of pages13
JournalZeitschrift für Rheumatologie
Volume80
Publication statusPublished - 12 Oct 2021
Peer-reviewedYes

External IDs

RIS Horneff2021
Scopus 85116893519
ORCID /0009-0003-6519-0482/work/143074874

Keywords

Keywords

  • Next-Generation-Sequenzierung, Panel-Sequenzierung, Whole-Exom-Sequenzierung, Whole-Genom-Sequenzierung, Hochdurchsatzsequenzierung, Next-generation sequencing, Panel sequencing, Whole exome sequencing, Whole genome sequencing, High-throughput sequencing